Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TMEFF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100509094:100509094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396G>T
AA Mutation	p.Gln132His(p.Q132H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100576526:100576526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139218600
CDS Mutation	c.1069A>C
AA Mutation	p.Lys357Gln(p.K357Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100516679:100516679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468G>T
AA Mutation	p.Glu156Asp(p.E156D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100547783:100547783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600T>G
AA Mutation	p.Asn200Lys(p.N200K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100572570:100572570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952C>T
AA Mutation	p.Leu318Phe(p.L318F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100576545:100576545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541170958
CDS Mutation	c.1088G>A
AA Mutation	p.Arg363Gln(p.R363Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100572522:100572522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>A
AA Mutation	p.Glu302Lys(p.E302K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374879
Start	100473697:100473697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMEFF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100547872:100547872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689G>T
AA Mutation	p.Arg230Met(p.R230M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100473575:100473575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>G
AA Mutation	p.Arg11Gly(p.R11G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100498853:100498853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285G>T
AA Mutation	p.Leu95Phe(p.L95F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100509088:100509088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390G>T
AA Mutation	p.Lys130Asn(p.K130N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374879
Start	100572558:100572558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940G>T
AA Mutation	p.Asp314Tyr(p.D314Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374879
Start	100576526:100576526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1073delA
AA Mutation	p.Asn358ThrfsTer11(p.N358Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000374879
Start	100561411:100561411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.790A>T
AA Mutation	p.Arg264Ter(p.R264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript